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Pharmacovigilance Opportunities at Parexel

In a Parexel Pharmacovigilance job, you’ll deliver patient safety services to help bio/pharmaceutical companies meet increasing safety obligations. You will support operational requirement changes, help lower safety monitoring costs, and ensure the team meets all regulatory requirements and post-authorization commitments. Help deliver the next generation of Pharmacovigilance services with a leader in product safety services and solutions. Explore Parexel careers.

Drug Safety Associate

Job ID 54633BR Hyderabad, Telangana, India
Assist in development of project specific safety procedures, workflows and templates
Assist in project specific safety database setup, development of data entry guidelines, and user acceptance testing
Triage incoming reports for completeness, legibility and validity
Electronic documentation and quality control of drug safety information
Data entry of case reports into safety database / tracking system
Request follow-up and perform query management
Coding of data in the safety database
Writing case narratives
Create and maintain project specific working files, case report files and project central files
Assist with additional Drug Safety Specialist on activities as required
Inform Line Manager (LM)/Team Manager, Safety Services Project Leader (SSPL) or Project Leader (PL) and Regional Head of PV Operations of potential change-in-scope of projects
Support of Medical Directors/Safety Physicians, as needed, in medical monitoring activities
Participate in client and investigator meetings as required
Attend internal, drug safety and project specific training sessions
Perform literature searches
Preparation for, participation in, and follow up on audits and inspections
Delegate work as appropriate to Drug Safety Assistants
Assistance in development of Expedited Reporting Procedures
Assistance with registration with relevant authorities for electronic reporting on behalf of sponsor
Assistance with setting up and deployment of worldwide reporting as required to regulatory authorities, CECs, local ECs, and investigator sites (electronic and hard copy)
Submission of safety reports to investigators via ISIS (International Safety Information System)
Assist with measuring investigative site performance in conducting required tasks in ISIS
Tracking and filing of submission cases as required
Assist with unblinding of SUSARs, as required
Support collection and review of metrics for measuring reporting compliance
Support Global Pharmacovigilance Information Office (GPIO) in the collection and organization of global PV requirements

Qualifications

Degree in Pharmacy, Nursing, Life Science or other health-related field, or equivalent qualification/work experience

Associates degree in any of the above with appropriate work experience of 1-2 years in Pharmacovigilance.

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